Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
  • C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
  • C07D317/44—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
  • C07D317/46—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with one six-membered ring
  • C07D317/48—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring
  • C07D317/62—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to atoms of the carbocyclic ring
  • C07D317/68—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
  • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
  • C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
  • C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
  • C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
  • C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D411/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen and sulfur atoms as the only ring hetero atoms
  • C07D411/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen and sulfur atoms as the only ring hetero atoms containing three or more hetero rings
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
  • C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
  • C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
  • C07D498/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains three hetero rings

Definitions

• the present invention relates to bicyclic bisamide derivatives, to processes for their preparation, to compositions comprising those compounds, and to their use for controlling insects or representatives of the order Acarina.
• Bisamide derivatives with insecticidal action are known and described, for example, in WO 2005/085234.
• G 1 , G 2 , and G 3 together with the two carbon atoms to which G 1 and G 3 are attached, form a non-aromatic 4- or 5-membered ring system; wherein G 1 is sulfur, SO, SO 2 , oxygen, a direct bond, NR a or CR 5a R 5b , G 2 is sulfur, SO, SO 2 , oxygen, a direct bond, NR b or CR 5c R 5d ; G 3 is sulfur, SO, SO 2 , oxygen, a direct bond, NR c or CR 5e R 5f ; with the provisos that a) not more than 1 group G can be a direct bond, b) not more than 2 G groups can be oxygen, sulfur, SO or SO 2 and c) when 2 G groups are oxygen, SO, SO 2 and/or sulfur the two groups are separated by a carbon atom; each of R 1a , R 1b , R 5a , R 5b , R 5c , R 5d R 5e ,
• R 4 , R 4 ′, R 10 , R 17 , and R 19 independently from each other, are hydrogen, C 1 -C 6 alkyl, C 3 -C 6 cycloalkyl, C 1 -C 6 haloalkyl, halogen, cyano, C 1 -C 4 alkoxy, C 1 -C 4 haloalkoxy, C 2 -C 4 alkoxycarbonyl, C 1 -C 4 alkylthio, C 1 -C 4 haloalkylthio, C 1 -C 4 alkylsulfonyl, C 1 -C 4 haloalkylsulfinyl or C 1 -C 4 haloalkylsulfonyl; R 5 , R 6 , R 8 , R 11 , R 12 , R 15 , R 16 and R 18 independently from each other, are C 1 -C 6 alkyl, or C 1 -C 6 cycloalkyl, C 1 -C 6
• Compounds I which have at least one basic centre can form, for example, acid addition salts, for example with strong inorganic acids such as mineral acids, for example perchloric acid, sulfuric acid, nitric acid, nitrose acid, a phosphorus acid or a hydrohalic acid, with strong organic carboxylic acids, such as C 1 -C 4 alkanecarboxylic acids which are unsubstituted or substituted, for example by halogen, for example acetic acid, such as saturated or unsaturated dicarboxylic acids, for example oxalic acid, malonic acid, succinic acid, maleic acid, fumaric acid or phthalic acid, such as hydroxycarboxylic acids, for example ascorbic acid, lactic acid, malic acid, tartaric acid or citric acid, or such as benzoic acid, or with organic sulfonic acids, such as C 1 -C 4 alkane- or arylsulfonic acids which are unsubstituted or substituted,
• Compounds I which have at least one acidic group can form, for example, salts with bases, for example mineral salts such as alkali metal or alkaline earth metal salts, for example sodium, potassium or magnesium salts, or salts with ammonia or an organic amine, such as morpholine, piperidine, pyrrolidine, a mono-, di- or tri-lower-alkylamine, for example ethyl-, diethyl-, triethyl- or dimethylpropylamine, or a mono-, di- or trihydroxy-lower-alkylamine, for example mono-, di- or triethanolamine.
• the corresponding internal salts can furthermore be formed.
• alkyl groups occurring in the definitions of the substituents can be straight-chain or branched and are, for example, methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, pentyl and hexyl and their branched isomers.
• Alkoxy, alkenyl and alkynyl radicals are derived from the alkyl radicals mentioned.
• the alkenyl and alkynyl groups can be mono- or polyunsaturated.
• Halogen is generally fluorine, chlorine, bromine or iodine. This also applies, correspondingly, to halogen in combination with other meanings, such as haloalkyl or halophenyl.
• Haloalkyl groups preferably have a chain length of from 1 to 6 carbon atoms.
• Haloalkyl is, for example, fluoromethyl, difluoromethyl, trifluoromethyl, chloromethyl, dichloromethyl, trichloromethyl, 2,2,2-trifluoroethyl, 2-fluoroethyl, 2-chloroethyl, pentafluoroethyl, 1,1-difluoro-2,2,2-trichloroethyl, 2,2,3,3-tetrafluoroethyl and 2,2,2-trichloroethyl; preferably trichloromethyl, difluorochloromethyl, difluoromethyl, trifluoromethyl and dichlorofluoromethyl.
• Suitable haloalkenyl groups are alkenyl groups which are mono- or polysubstituted by halogen, halogen being fluorine, chlorine, bromine and iodine and in particular fluorine and chlorine, for example 2,2-difluoro-1-methylvinyl, 3-fluoropropenyl, 3-chloropropenyl, 3-bromopropenyl, 2,3,3-trifluoropropenyl, 2,3,3-trichloropropenyl and 4,4,4-trifluorobut-2-en-1-yl.
• halogen being fluorine, chlorine, bromine and iodine and in particular fluorine and chlorine, for example 2,2-difluoro-1-methylvinyl, 3-fluoropropenyl, 3-chloropropenyl, 3-bromopropenyl, 2,3,3-trifluoropropenyl, 2,3,3-trichloropropenyl and 4,4,4-trifluorobut-2-
• Suitable haloalkynyl groups are, for example, alkynyl groups which are mono- or polysubstituted by halogen, halogen being bromine, iodine and in particular fluorine and chlorine, for example 3-fluoropropynyl, 3-chloropropynyl, 3-bromopropynyl, 3,3,3-trifluoropropynyl and 4,4,4-trifluorobut-2-yn-1-yl.
• alkynyl groups which are mono- or polysubstituted by halogen preference is given to those having chain length of from 3 to 5 carbon atoms.
• Alkoxy groups preferably have a preferred chain length of from 1 to 6 carbon atoms.
• Alkoxy is, for example, methoxy, ethoxy, propoxy, i-propoxy, n-butoxy, isobutoxy, sec-butoxy and tert-butoxy and also the isomeric pentyloxy and hexyloxy radicals; preferably methoxy and ethoxy.
• Alkoxycarbonyl is, for example, methoxycarbonyl, ethoxycarbonyl, propoxycarbonyl, isopropoxycarbonyl, n-butoxycarbonyl, isobutoxycarbonyl, sec-butoxycarbonyl or tert-butoxycarbonyl; preferably methoxycarbonyl or ethoxycarbonyl.
• Haloalkoxy groups preferably have a chain length of from 1 to 6 carbon atoms.
• Haloalkoxy is, for example, fluoromethoxy, difluoromethoxy, trifluoromethoxy, 2,2,2-trifluoroethoxy, 1,1,2,2-tetrafluoroethoxy, 2-fluoroethoxy, 2-chloroethoxy, 2,2-difluoroethoxy and 2,2,2-trichloroethoxy; preferably difluoromethoxy, 2-chloroethoxy and trifluoromethoxy.
• Alkylthio groups preferably have a chain length of from 1 to 6 carbon atoms.
• Alkylthio is, for example, methylthio, ethylthio, propylthio, isopropylthio, n-butylthio, isobutylthio, sec-butylthio or tert-butylthio, preferably methylthio and ethylthio.
• Alkylsulfinyl is, for example, methylsulfinyl, ethylsulfinyl, propylsulfinyl, isopropylsulfinyl, n-butylsulfinyl, isobutylsulfinyl, sec-butylsulfinyl, tert-butylsulfinyl; preferably methylsulfinyl and ethylsulfinyl.
• Alkylsulfonyl is, for example, methylsulfonyl, ethylsulfonyl, propylsulfonyl, isopropylsulfonyl, n-butylsulfonyl, isobutylsulfonyl, sec-butylsulfonyl or tert-butylsulfonyl; preferably methylsulfonyl or ethylsulfonyl.
• Alkylamino is, for example, methylamino, ethylamino, n-propylamino, isopropylamino or the isomeric butylamines.
• Dialkylamino is, for example, dimethylamino, methylethylamino, diethylamino, n-propylmethylamino, dibutylamino and diisopropylamino.
• Preference is given to alkylamino groups having a chain length of from 1 to 4 carbon atoms.
• Alkoxyalkyl groups preferably have a chain length of 1 to 6 carbon atoms.
• Alkoxyalkyl is, for example, methoxymethyl, methoxyethyl, ethoxymethyl, ethoxyethyl, n-propoxymethyl, n-propoxyethyl, isopropoxymethyl or isopropoxyethyl.
• Alkylthioalkyl groups preferably have from 1 to 8 carbon atoms.
• Alkylthioalkyl is, for example, methylthiomethyl, methylthioethyl, ethylthiomethyl, ethylthioethyl, n-propylthiomethyl, n-propylthioethyl, isopropylthiomethyl, isopropylthioethyl, butylthiomethyl, butylthioethyl or butylthiobutyl.
• the cycloalkyl groups preferably have from 3 to 6 ring carbon atoms, for example cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl.
• Phenyl also as part of a substituent such as phenoxy, benzyl, benzyloxy, benzoyl, phenylthio, phenylalkyl, phenoxyalkyl, may be substituted.
• the substituents can be in ortho, meta and/or para position.
• the preferred substituent positions are the ortho and para positions to the ring attachment point.
• a three- to ten-membered monocyclic or fused bicyclic ring system which may be aromatic, partially saturated or fully saturated is, depending of the number of ring members, for example, selected from the group consisting of
• each R 26 is methyl
• each R 27 and each R 28 are independently hydrogen, C 1 -C 3 alkyl, C 1 -C 3 alkoxy, C 1 -C 3 alkylthio or trifluoromethyl
• X 4 is oxygen or sulfur and r is 1, 2, 3 or 4.
• the linkage site is located at the carbon atom labelled “CH” or in a case such as, for example,
• Z 1 and/or Z 2 are oxygen.
• R 2 and/or R 3 is hydrogen.
• R 20 is preferably hydrogen, methyl, ethyl, i-propyl, tert.-butyl, CH 2 —C 3 H 5 , C(CH 2 CH 2 )—C 3 H 5 , C(CH 3 ) 2 CH 2 SCH 3 , C(CH 3 ) 2 CH 2 S(O)CH 3 , C(CH 3 ) 2 CH 2 S(O) 2 CH 3 , CH 2 CN, CH(CH 3 )CH 3 SCH 3 , CH(CH 3 )CH 3 S(O)CH 3 or CH(CH 3 )CH 3 S(O) 2 CH 3 , 3-methyl-thietan-3-yl, 1-oxo-3-methyl-thietan-3-yl or 1,1-dioxo-3-methyl-thietan-3-yl, in particular hydrogen, methyl, ethyl, i-propyl, tert.-butyl, CH 2 —C 3 H 5 , C(CH 2 CH 2 )—
• D is preferably a group D 1 , wherein R 4 ′ is hydrogen, R 5 is 2-pyridyl which can be substituted by halogen, preferably which is monosubstituted by chloro at the 3-position of the pyridine ring and R 4 is halogen preferably chloro or bromo, C 1 -C 6 haloalkyl, C 1 -C 4 alkoxy, C 1 -C 4 haloalkoxy most preferably OCH 3 , OCF 2 H or 2,2,2-trifluoroethoxy, preferably C 1 -C 6 haloalkyl, most preferably trifluoromethyl.
• each of R 1a and R 1b which may be the same or different, represents hydrogen, halogen, cyano, hydroxy, CHO, C 1 -C 6 alkyl, C 3 -C 6 cycloalkyl, C 1 -C 6 haloalkyl, C 1 -C 4 alkoxy, C 1 -C 4 alkoxy-C 1 -C 4 alkoxy-C 1 -C 4 alkyl, C 1 -C 4 alkylthio, C 1 -C 4 alkylsulfinyl, C 1 -C 4 alkylsulfonyl, C 1 -C 4 alkylsulfonyl-C 1 -C 4 alkyl, C 1 -C 4 alkylsulfoximino-C 1 -C 4 alkyl, C 2 -C 4 dialkylamino or C 1 -C 4 alkoxyimino-C 1 -C 4 alkyl.
• each of G 1 , G 2 and G 3 which may be the same or different, represents NH, O, S, SO, SO 2 , CR 5a R 5b , CR 5c R 5d or CR 5e R 5f wherein each of R 5a , R 5b , R 6c , R 5d , R 5e and R 5f which may be the same or different represents hydrogen, halogen, cyano, hydroxy, CHO, C 1 -C 6 alkyl, C 3 -C 6 cycloalkyl, C 1 -C 6 haloalkyl, C 1 -C 4 alkoxy, C 1 -C 4 alkoxy-C 1 -C 4 alkoxy-C 1 -C 4 alkyl, C 1 -C 4 alkylthio, C 1 -C 4 alkylsulfinyl, C 1 -C 4 alkylsulfonyl, C 1 -C 4 alkylsulfonyl-C 1 -C 1
• R 101 is halogen, C 1 -C 4 haloalkyl, C 1 -C 4 haloalkoxy, C 1 -C 4 alkoxy, especially difluoromethyl, trifluoromethyl, chlorine, bromine, OCF 2 H, O—CH 2 —CF 3 or OCH 3 , in particular halogen, haloalkyl, haloalkoxy, especially trifluoromethyl, chlorine, bromine, OCF 2 H, OCH 3 , or O—CH 2 —CF 3 ;
• R 102 is hydrogen, halogen, C 1 -C 6 -alkyl, C 2 -C 6 -alkynyl, cyano, especially methyl, ethynyl, chlorine or bromine; in particular halogen, C 1 -C 6 -alkyl, especially methyl, chlorine or bromine; and
• R 103 is hydrogen, methyl, ethyl,
• R 1a is hydrogen, C 1 -C 4 alkyl, C 2 -C 4 alkynyl, halogen or cyano
• R 20 is hydrogen, C 1 -C 6 alkyl, C 1 -C 6 alkylthio-C 1 -C 6 alkyl, C 1 -C 6 alkylsulfonyl-C 1 -C 6 alkyl, C 1 -C 6 alkylsulfinyl-C 1 -C 6 alkyl, thiethan-3-yl, thiethan-3-yl substituted by C 1 -C 4 alkyl, preferably 3-methyl-thietan-3-yl,
• C 1 -C 6 alkyl in particular hydrogen, C 1 -C 6 alkyl, C 1 -C 6 alkylthio-C 1 -C 6 alkyl, C 1 -C 6 alkylsulfonyl-C 1 -C 6 alkyl, C 1 -C 6 alkylsulfinyl-C 1 -C 6 alkyl,
• R 100 is halogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 alkoxy or C 1 -C 6 haloalkoxy; in particular halogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl or C 1 -C 6 alkoxy.
• R 1a is hydrogen, C 1 -C 4 alkyl, C 2 -C 4 alkynyl, halogen or cyano; in particular chloro or methyl;
• R 20 is hydrogen, C 1 -C 6 alkyl, C 1 -C 6 alkylthio-C 1 -C 6 alkyl, C 1 -C 6 alkylsulfonyl-C 1 -C 6 alkyl, C 1 -C 6 alkylsulfinyl-C 1 -C 6 alkyl, thiethan-3-yl, thiethan-3-yl substituted by C 1 -C 4 alkyl, preferably 3-methyl-thietan-3-yl,
• C 1 -C 6 alkyl in particular hydrogen, C 1 -C 6 alkyl, C 1 -C 6 alkylthio-C 1 -C 6 alkyl, C 1 -C 6 alkylsulfonyl-C 1 -C 6 alkyl, C 1 -C 6 alkylsulfinyl-C 1 -C 6 alkyl,
• R 100 is halogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 alkoxy or C 1 -C 6 haloalkoxy; in particular halogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl or C 1 -C 6 haloalkoxy; in particular trifluoromethyl, difluoromethyl, methoxy, bromo, chloro or 1,1,1-trifluoroethoxy.
• embodiment E1 is represented by the compounds of formula T1
• R 1a is hydrogen, C 1 -C 4 alkyl, C 2 -C 4 alkynyl, halogen or cyano; in particular chloro or methyl;
• R 20 is hydrogen, C 1 -C 6 alkyl, C 1 -C 6 alkylthio-C 1 -C 6 alkyl, C 1 -C 6 alkylsulfonyl-C 1 -C 6 alkyl, C 1 -C 6 alkylsulfinyl-C 1 -C 6 alkyl, thiethan-3-yl, thiethan-3-yl substituted by C 1 -C 4 alkyl, preferably 3-methyl-thietan-3-yl,
• C 1 -C 6 alkyl in particular hydrogen, C 1 -C 6 alkyl, C 1 -C 6 alkylthio-C 1 -C 6 alkyl, C 1 -C 6 alkylsulfonyl-C 1 -C 6 alkyl, C 1 -C 6 alkylsulfinyl-C 1 -C 6 alkyl,
• R 100 is halogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 alkoxy or C 1 -C 6 haloalkoxy; in particular halogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl or C 1 -C 6 haloalkoxy; in particular trifluoromethyl, difluoromethyl, methoxy, bromo, chloro or 1,1,1-trifluoroethoxy.
• Embodiments E2 to E55 are defined accordingly.
• B 1 is H, Cl, Br, I or C1-6 alkyl and B 2 and B 3 are each independently H or F are novel. Examples of such compounds are given in Table B
• LC/MS data are obtained using a ZMD Mass Spectrometer from Waters (Single quadrupole mass spectrometer).
• Ionisation method Electrospray; and HPLC from Agilent: quaternary HPLC pump HP1100, HP1100 Variable Wavelength Detector, HP1100 thermostatted column compartment and HP1100 solvent degasser.
• Table C1 This table discloses the 21 compounds C1.1 to C1.21 of the formula TC1
• variable R 201 has the specific meaning given in the corresponding line, appropriately selected from the 21 lines C.1.1 to C.1.21 of the Table C.
• the compounds of formula TC1, wherein R 201 is C 5 -C 12 alkyl, cyclohexyl, allyl, pentafluorophenyl, 2-nitrophenyl, 4-nitrophenyl or 2,4-dinitrophenyl are novel and as such form a further aspect of the invention.
• Table C2 This table discloses the 21 compounds C2.1 to C2.21 of the formula TC2
• variable R 201 has the specific meaning given in the corresponding line, appropriately selected from the 21 lines C.2.1 to C.2.21 of the table C.
• the compounds of formula TC2, wherein R 201 is C 5 -C 12 alkyl, cyclohexyl, allyl, pentafluorophenyl, 2-nitrophenyl, 4-nitrophenyl or 2,4-dinitrophenyl are novel and as such form a further aspect of the invention.
• Table C3 This table discloses the 21 compounds C3.1 to C3.21 of the formula TC3
• variable R 201 has the specific meaning given in the corresponding line, appropriately selected from the 21 lines C.3.1 to C.3.21 of the table C.
• the compounds of formula TC3, wherein R 201 is C 5 -C 12 alkyl, cyclohexyl, allyl, pentafluorophenyl, 2-nitrophenyl, 4-nitrophenyl or 2,4-dinitrophenyl are novel and as such form a further aspect of the invention.
• Table C4 This table discloses the 21 compounds C4.1 to C4.21 of the formula TC4
• variable R 201 has the specific meaning given in the corresponding line, appropriately selected from the 21 lines C.4.1 to C.4.21 of the table C.
• the compounds of formula TC4, wherein R 201 is C 5 -C 12 alkyl, cyclohexyl, allyl, pentafluorophenyl, 2-nitrophenyl, 4-nitrophenyl or 2,4-dinitrophenyl are novel and as such form a further aspect of the invention.
• Table C5 This table discloses the 21 compounds C5.1 to C5.21 of the formula TC5
• variable R 201 has the specific meaning given in the corresponding line, appropriately selected from the 21 lines C.5.1 to C.5.21 of the table C.
• the compounds of formula TC5, wherein R 201 is C 5 -C 12 alkyl, cyclohexyl, allyl, pentafluorophenyl, 2-nitrophenyl, 4-nitrophenyl or 2,4-dinitrophenyl are novel and as such form a further aspect of the invention.
• Table C6 This table discloses the 21 compounds C6.1 to C6.21 of the formula TC6
• variable R 201 has the specific meaning given in the corresponding line, appropriately selected from the 21 lines C.6.1 to C.6.21 of the table C.
• the compounds of formula TC6, wherein R 201 is C 5 -C 12 alkyl, cyclohexyl, allyl, pentafluorophenyl, 2-nitrophenyl, 4-nitrophenyl or 2,4-dinitrophenyl are novel and as such form a further aspect of the invention.
• Table C7 This table discloses the 21 compounds C7.1 to C7.21 of the formula TC7
• variable R 201 has the specific meaning given in the corresponding line, appropriately selected from the 21 lines C.7.1 to C.7.21 of the table C.
• the compounds of formula TC7, wherein R 201 is C 5 -C 12 alkyl, cyclohexyl, allyl, pentafluorophenyl, 2-nitrophenyl, 4-nitrophenyl or 2,4-dinitrophenyl are novel and as such form a further aspect of the invention.
• Table C8 This table discloses the 21 compounds C8.1 to C8.21 of the formula TC8
• variable R 201 has the specific meaning given in the corresponding line, appropriately selected from the 21 lines C.8.1 to C.8.21 of the table C.
• the compounds of formula TC8, wherein R 201 is C 5 -C 12 alkyl, cyclohexyl, allyl, pentafluorophenyl, 2-nitrophenyl, 4-nitrophenyl or 2,4-dinitrophenyl are novel and as such form a further aspect of the invention.
• Table C9 This table discloses the 21 compounds C9.1 to C9.21 of the formula TC9
• variable R 201 has the specific meaning given in the corresponding line, appropriately selected from the 21 lines C.9.1 to C.9.21 of the table C.
• the compounds of formula TC9, wherein R 201 is C 5 -C 12 alkyl, cyclohexyl, allyl, pentafluorophenyl, 2-nitrophenyl, 4-nitrophenyl or 2,4-dinitrophenyl are novel and as such form a further aspect of the invention.
• Table C10 This table discloses the 21 compounds C10.1 to C10.21 of the formula TC10
• variable R 201 has the specific meaning given in the corresponding line, appropriately selected from the 21 lines C.10.1 to C.10.21 of the table C.
• Table C11 This table discloses the 21 compounds C11.1 to C11.21 of the formula TC11
• variable R 201 has the specific meaning given in the corresponding line, appropriately selected from the 21 lines C.11.1 to C.11.21 of the table C.
• Table C12 This table discloses the 21 compounds C12.1 to C12.21 of the formula TC12
• variable R201 has the specific meaning given in the corresponding line, appropriately selected from the 21 lines C.12.1 to C.12.21 of the table C.
• Certain compounds of Table C12 are novel and as such form a further aspect of the invention.
• Compounds C12.4, C12.6, C12.8, C12.16 and C12.18 are known compounds.
• Table C13 This table discloses the 21 compounds C13.1 to C13.21 of the formula TC13
• variable R 201 has the specific meaning given in the corresponding line, appropriately selected from the 21 lines C.13.1 to C.13.21 of the table C.
• the compounds of Table C13 are novel and as such form a further aspect of the invention.
• Table D1 This table discloses the 84 compounds D1.1 to D1.84 of the formula TD1
• each of the of the variables R 201 and R 202 has the specific meaning given in the corresponding line, appropriately selected from the 84 lines D.1.1 to D.1.84 of the Table D.
• Table E1 This table discloses the 4 compounds E1.1 to E1.4 of the formula TE1
• variable R 202 has the specific meaning given in the corresponding line, appropriately selected from the 4 lines E.1.1 to E.1.4 of the Table E.
• R 1a , R 1b , G 1 , G 2 , G 3 and R 2 are as define above.
• the reactants can be reacted in the presence of a base.
• suitable bases are alkali metal or alkaline earth metal hydroxides, alkali metal or alkaline earth metal hydrides, to alkali metal or alkaline earth metal amides, alkali metal or alkaline earth metal alkoxides, alkali metal or alkaline earth metal acetates, alkali metal or alkaline earth metal carbonates, alkali metal or alkaline earth metal dialkylamides or alkali metal or alkaline earth metal alkylsilylamides, alkylamines, alkylenediamines, free or N-alkylated saturated or unsaturated cycloalkylamines, basic heterocycles, ammonium hydroxides and carbocyclic amines.
• Examples which may be mentioned are sodium hydroxide, sodium hydride, sodium amide, sodium methoxide, sodium acetate, sodium carbonate, potassium tert-butoxide, potassium hydroxide, potassium carbonate, potassium hydride, lithium diisopropylamide, potassium bis(trimethylsilyl)amide, calcium hydride, triethylamine, diisopropylethylamine, triethylenediamine, cyclohexylamine, N-cyclohexyl-N,N-dimethylamine, N,N-diethylaniline, pyridine, 4-(N,N-dimethylamino)pyridine, quinuclidine, N-methylmorpholine, benzyltrimethylammonium hydroxide and 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU).
• DBU 1,8-diazabicyclo[5.4.0]undec-7-ene
• the reactants can be reacted with each other as such, i.e. without adding a solvent or diluent. In most cases, however, it is advantageous to add an inert solvent or diluent or a mixture of these. If the reaction is carried out in the presence of a base, bases which are employed in excess, such as triethylamine, pyridine, N-methylmorpholine or N,N-diethylaniline, may also act as solvents or diluents.
• the reaction is advantageously carried out in a temperature range from approximately ⁇ 80° C. to approximately +140° C., preferably from approximately ⁇ 30° C. to approximately +100° C., in many cases in the range between ambient temperature and approximately +80° C.
• a compound I can be converted in a manner known per se into another compound I by replacing one or more substituents of the starting compound I in the customary manner by (an)other substituent(s) according to the invention.
• Salts of compounds I can be prepared in a manner known per se.
• acid addition salts of compounds I are obtained by treatment with a suitable acid or a suitable ion exchanger reagent and salts with bases are obtained by treatment with a suitable base or with a suitable ion exchanger reagent.
• Salts of compounds I can be converted in the customary manner into the free compounds I, acid addition salts, for example, by treatment with a suitable basic compound or with a suitable ion exchanger reagent and salts with bases, for example, by treatment with a suitable acid or with a suitable ion exchanger reagent.
• Salts of compounds I can be converted in a manner known per se into other salts of compounds I, acid addition salts, for example, into other acid addition salts, for example by treatment of a salt of inorganic acid such as hydrochloride with a suitable metal salt such as a sodium, barium or silver salt, of an acid, for example with silver acetate, in a suitable solvent in which an inorganic salt which forms, for example silver chloride, is insoluble and thus precipitates from the reaction mixture.
• a salt of inorganic acid such as hydrochloride
• a suitable metal salt such as a sodium, barium or silver salt
• the compounds I which have salt-forming properties can be obtained in free form or in the form of salts.
• the compounds I and, where appropriate, the tautomers thereof, in each case in free form or in salt form, can be present in the form of one of the isomers which are possible or as a mixture of these, for example in the form of pure isomers, such as antipodes and/or diastereomers, or as isomer mixtures, such as enantiomer mixtures, for example racemates, diastereomer mixtures or racemate mixtures, depending on the number, absolute and relative configuration of asymmetric carbon atoms which occur in the molecule and/or depending on the configuration of non-aromatic double bonds which occur in the molecule; the invention relates to the pure isomers and also to all isomer mixtures which are possible and is to be understood in each case in this sense hereinabove and hereinbelow, even when stereochemical details are not mentioned specifically in each case.
• Diastereomer mixtures or racemate mixtures of compounds I, in free form or in salt form, which can be obtained depending on which starting materials and procedures have been chosen can be separated in a known manner into the pure diasteromers or racemates on the basis of the physicochemical differences of the components, for example by fractional crystallization, distillation and/or chromatography.
• Enantiomer mixtures such as racemates, which can be obtained in a similar manner can be resolved into the optical antipodes by known methods, for example by recrystallization from an optically active solvent, by chromatography on chiral adsorbents, for example high-performance liquid chromatography (HPLC) on acetyl cellulose, with the aid of suitable microorganisms, by cleavage with specific, immobilized enzymes, via the formation of inclusion compounds, for example using chiral crown ethers, where only one enantiomer is complexed, or by conversion into diastereomeric salts, for example by reacting a basic end-product racemate with an optically active acid, such as a carboxylic acid, for example camphor, tartaric or malic acid, or sulfonic acid, for example camphorsulfonic acid, and separating the diastereomer mixture which can be obtained in this manner, for example by fractional crystallization based on their differing solubilities, to give the di
• Pure diastereomers or enantiomers can be obtained according to the invention not only by separating suitable isomer mixtures, but also by generally known methods of diastereoselective or enantioselective synthesis, for example by carrying out the process according to the invention with starting materials of a suitable stereochemistry.
• the compounds I and, where appropriate, the tautomers thereof, in each case in free form or in salt form, can, if appropriate, also be obtained in the form of hydrates and/or include other solvents, for example those which may have been used for the crystallization of compounds which are present in solid form.
• the compounds I according to the invention are preventively and/or curatively valuable active ingredients in the field of pest control, even at low rates of application, which have a very favorable biocidal spectrum and are well tolerated by warm-blooded species, fish and plants.
• the active ingredients according to the invention act against all or individual developmental stages of normally sensitive, but also resistant, animal pests, such as insects or representatives of the order Acarina.
• the insecticidal or acaricidal activity of the active ingredients according to the invention can manifest itself directly, i.e.
• Tetranychus spp. from the order Anoplura, for example, Haematopinus spp., Linognathus spp., Pediculus spp., Pemphigus spp. and Phylloxera spp.; from the order Coleoptera, for example, Agriotes spp., Anthonomus spp., Atomaria linearis, Chaetocnema tibialis, Cosmopolites spp., Curculio spp., Dermestes spp., Diabrotica spp., Epilachna spp., Eremnus spp., Leptinotarsa decemLineata, Lissorhoptrus spp., Melolontha spp., Orycaephilus spp., Otiorhynchus spp., Phlyctinus spp., Popillia spp., Psy
• Trogoderma spp. from the order Diptera, for example, Aedes spp., Antherigona soccata, Bibio hortulanus, Calliphora erythrocephala, Ceratitis spp., Chrysomyia spp., Culex spp., Cuterebra spp., Dacus spp., Drosophila melanogaster, Fannia spp., Gastrophilus spp., Glossina spp., Hypoderma spp., Hyppobosca spp., Liriomyza spp., Lucilia spp., Melanagromyza spp., Musca spp., Oestrus spp., Orseolia spp., Oscinella frit, Pegomyia hyoscyami, Phorbia spp., Rhagoletis pomonella, Sciara spp., Stor
• Tipula spp. from the order Heteroptera, for example, Cimex spp., Distantiella theobroma, Dysdercus spp., Euchistus spp., Eurygaster spp., Leptocorisa spp., Nezara spp., Piesma spp., Rhodnius spp., Sahlbergella singularis, Scotinophara spp.
• Triatoma spp. from the order Homoptera, for example, Aleurothrixus floccosus, Aleyrodes brassicae, Aonidiella spp., Aphididae, Aphis spp., Aspidiotus spp., Bemisia tabaci, Ceroplaster spp., Chrysomphalus aonidium, Chrysomphalus dictyospermi, Coccus hesperidum, Empoasca spp., Eriosoma larigerum, Erythroneura spp., Gascardia spp., Laodelphax spp., Lecanium corni, Lepidosaphes spp., Macrosiphus spp., Myzus spp., Nephotettix spp., Nilaparvata spp., Parlatoria spp., Pemphigus spp., Planococc
• Vespa spp. from the order Isoptera, for example, Reticulitermes spp.; from the order Lepidoptera, for example, Acleris spp., Adoxophyes spp., Aegeria spp., Agrotis spp., Alabama argillaceae, Amylois spp., Anticarsia gemmatalis, Archips spp., Argyrotaenia spp., Autographa spp., Busseola fusca, Cadra cautella, Carposina nipponensis, Chilo spp., Choristoneura spp., Clysia ambiguella, Cnaphalocrocis spp., Cnephasia spp., Cochylis spp., Coleophora spp., Crocidolomia binotalis, Cryptophlebia leucotreta, Cydia spp., Diatraea s
• Trichodectes spp. from the order Orthoptera, for example, Blatta spp., Blattella spp., Gryllotalpa spp., Leucophaea maderae, Locusta spp., Periplaneta spp. and Schistocerca spp.; from the order Psocoptera, for example, Liposcelis spp.; from the order Siphonaptera, for example, Ceratophyllus spp., Ctenocephalides spp.
• Thysanoptera for example, Frankliniella spp., Hercinothrips spp., Scirtothrips aurantii, Taeniothrips spp., Thrips palmi and Thrips tabaci ; and from the order Thysanura, for example, Lepisma saccharina.
• the active ingredients according to the invention can be used for controlling, i.e. containing or destroying, pests of the abovementioned type which occur in particular on plants, especially on useful plants and ornamentals in agriculture, in horticulture and in forests, or on organs, such as fruits, flowers, foliage, stalks, tubers or roots, of such plants, and in some cases even plant organs which are formed at a later point in time remain protected against these pests.
• Suitable target crops are, in particular, cereals, such as wheat, barley, rye, oats, rice, maize or sorghum; beet, such as sugar or fodder beet; fruit, for example pomaceous fruit, stone fruit or soft fruit, such as apples, pears, plums, peaches, almonds, cherries or berries, for example strawberries, raspberries or blackberries; leguminous crops, such as beans, lentils, peas or soya; oil crops, such as oilseed rape, mustard, poppies, olives, sunflowers, coconut, castor, cocoa or ground nuts; cucurbits, such as pumpkins, cucumbers or melons; fibre plants, such as cotton, flax, hemp or jute; citrus fruit, such as oranges, lemons, grapefruit or tangerines; vegetables, such as spinach, lettuce, asparagus, cabbages, carrots, onions, tomatoes, potatoes or bell peppers; Lauraceae, such as avocado, Cinnamonium or camphor; and also tobacco, nuts,
• the active ingredients according to the invention are especially suitable for controlling Aphis craccivora, Diabrotica balteata, Heliothis virescens, Myzus persicae, Plutella xylostella and Spodoptera littoralis in cotton, vegetable, maize, rice and soya crops.
• the active ingredients according to the invention are further especially suitable for controlling Mamestra (preferably in vegetables), Cydia pomonella (preferably in apples), Empoasca (preferably in vegetables, vineyards), Leptinotarsa (preferably in potatoes) and Chilo supressalis (preferably in rice).
• crops is to be understood as including also crops that have been rendered tolerant to herbicides like bromoxynil or classes of herbicides (such as, for example, HPPD inhibitors, ALS inhibitors, for example primisulfuron, prosulfuron and trifloxysulfuron, EPSPS (5-enol-pyrovyl-shikimate-3-phosphate-synthase) inhibitors, GS (glutamine synthetase) inhibitors) as a result of conventional methods of breeding or genetic engineering.
• herbicides like bromoxynil or classes of herbicides
• ALS inhibitors for example primisulfuron, prosulfuron and trifloxysulfuron
• EPSPS 5-enol-pyrovyl-shikimate-3-phosphate-synthase
• GS glutamine synthetase
• imazamox by conventional methods of breeding (mutagenesis) is Clearfield® summer rape (Canola).
• crops that have been rendered tolerant to herbicides or classes of herbicides by genetic engineering methods include glyphosate- and glufosinate-resistant maize varieties commercially available under the trade names RoundupReady® and LibertyLink®.
• crops is to be understood as including also crop plants which have been so transformed by the use of recombinant DNA techniques that they are capable of synthesising one or more selectively acting toxins, such as are known, for example, from toxin-producing bacteria, especially those of the genus Bacillus.
• Toxins that can be expressed by such transgenic plants include, for example, insecticidal proteins, for example insecticidal proteins from Bacillus cereus or Bacillus popliae ; or insecticidal proteins from Bacillus thuringiensis , such as ⁇ -endotoxins, e.g. CryIA(b), CryIA(c), CryIF, CryIF(a2), CryIIA(b), CryIIIA, CryIIIB(b1) or Cry9c, or vegetative insecticidal proteins (VIP), e.g. VIP1, VIP2, VIP3 or VIP3A; or insecticidal proteins of bacteria colonising nematodes, for example Photorhabdus spp.
• insecticidal proteins for example insecticidal proteins from Bacillus cereus or Bacillus popliae
• Bacillus thuringiensis such as ⁇ -endotoxins, e.g. CryIA(b), CryIA(c), CryIF, C
• Xenorhabdus spp. such as Photorhabdus luminescens, Xenorhabdus nematophilus ; toxins produced by animals, such as scorpion toxins, arachnid toxins, wasp toxins and other insect-specific neurotoxins; toxins produced by fungi, such as Streptomycetes toxins, plant lectins, such as pea lectins, barley lectins or snowdrop lectins; agglutinins; proteinase inhibitors, such as trypsine inhibitors, serine protease inhibitors, patatin, cystatin, papain inhibitors; ribosome-inactivating proteins (RIP), such as ricin, maize-RIP, abrin, luffin, saporin or bryodin; steroid metabolism enzymes, such as 3-hydroxysteroidoxidase, ecdysteroid-UDP-glycosyltransferase, cholesterol oxidases, ecd
• ⁇ -endotoxins for example CryIA(b), CryIA(c), CryIF, CryIF(a2), CryIIA(b), CryIIIA, CryIIIB(b1) or Cry9c, or vegetative insecticidal proteins (VIP), for example VIP1, VIP2, VIP3 or VIP3A
• VIP vegetative insecticidal proteins
• Hybrid toxins are produced recombinantly by a new combination of different domains of those proteins (see, for example, WO 02/15701).
• Truncated toxins for example a truncated CryIA(b), are known.
• modified toxins one or more amino acids of the naturally occurring toxin are replaced.
• amino acid replacements preferably non-naturally present protease recognition sequences are inserted into the toxin, such as, for example, in the case of CryIIIA055, a cathepsin-D-recognition sequence is inserted into a CryIIIA toxin (see WO 03/018810).
• Examples of such toxins or transgenic plants capable of synthesising such toxins are disclosed, for example, in EP-A-0 374 753, WO 93/07278, WO 95/34656, EP-A-0 427 529, EP-A-451 878 and WO 03/052073.
• the toxin contained in the transgenic plants imparts to the plants tolerance to harmful insects.
• insects can occur in any taxonomic group of insects, but are especially commonly found in the beetles (Coleoptera), two-winged insects (Diptera) and butterflies (Lepidoptera).
• Transgenic plants containing one or more genes that code for an insecticidal resistance and express one or more toxins are known and some of them are commercially available. Examples of such plants are: YieldGard® (maize variety that expresses a CryIA(b) toxin); YieldGard Rootworm® (maize variety that expresses a CryIIIB(b1) toxin); YieldGard Plus® (maize variety that expresses a CryIA(b) and a CryIIIB(b1) toxin); Starlink® (maize variety that expresses a Cry9(c) toxin); Herculex I® (maize variety that expresses a CryIF(a2) toxin and the enzyme phosphinothricine N-acetyltransferase (PAT) to achieve tolerance to the herbicide glufosinate ammonium); NuCOTN 33B® (cotton variety that expresses a CryIA(c) toxin
• transgenic crops are:
• MIR604 Maize from Syngenta Seeds SAS, Chemin de l'Hobit 27, F-31 790 St. Sauveur, France, registration number C/FR/96/05/10. Maize which has been rendered insect-resistant by transgenic expression of a modified CryIIIA toxin. This toxin is Cry3A055 modified by insertion of a cathepsin-D-protease recognition sequence. The preparation of such transgenic maize plants is described in WO 03/018810.
• MON 863 Maize from Monsanto Europe S.A. 270-272 Avenue de Tervuren, B-1150 Brussels, Belgium, registration number C/DE/02/9. MON 863 expresses a CryIIIB(b1) toxin and has resistance to certain Coleoptera insects.
• NK603 ⁇ MON 810 Maize from Monsanto Europe S.A. 270-272 Avenue de Tervuren, B-1150 Brussels, Belgium, registration number C/GB/02/M3/03. Consists of conventionally bred hybrid maize varieties by crossing the genetically modified varieties NK603 and MON 810.
• NK603 ⁇ MON 810 Maize transgenically expresses the protein CP4 EPSPS, obtained from Agrobacterium sp. strain CP4, which imparts tolerance to the herbicide Roundup® (contains glyphosate), and also a CryIA(b) toxin obtained from Bacillus thuringiensis subsp. kurstaki which brings about tolerance to certain Lepidoptera, include the European corn borer.
• crops is to be understood as including also crop plants which have been so transformed by the use of recombinant DNA techniques that they are capable of synthesising antipathogenic substances having a selective action, such as, for example, the so-called “pathogenesis-related proteins” (PRPs, see e.g. EP-A-0 392 225).
• PRPs pathogenesis-related proteins
• Examples of such antipathogenic substances and transgenic plants capable of synthesising such antipathogenic substances are known, for example, from EP-A-0 392 225, WO 95/33818 and EP-A-0 353 191.
• the methods of producing such transgenic plants are generally known to the person skilled in the art and are described, for example, in the publications mentioned above.
• Antipathogenic substances which can be expressed by such transgenic plants include, for example, ion channel blockers, such as blockers for sodium and calcium channels, for example the viral KP1, KP4 or KP6 toxins; stilbene synthases; bibenzyl synthases; chitinases; glucanases; the so-called “pathogenesis-related proteins” (PRPs; see e.g. EP-A-0 392 225); antipathogenic substances produced by microorganisms, for example peptide antibiotics or heterocyclic antibiotics (see e.g. WO 95/33818) or protein or polypeptide factors involved in plant pathogen defence (so-called “plant disease resistance genes”, as described in WO 03/000906).
• ion channel blockers such as blockers for sodium and calcium channels
• the viral KP1, KP4 or KP6 toxins stilbene synthases; bibenzyl synthases; chitinases; glucanases; the so-called “pathogenesis
• compositions according to the invention are the protection of stored goods and storerooms and the protection of raw materials, such as wood, textiles, floor coverings or buildings, and also in the hygiene sector, especially the protection of humans, domestic animals and productive livestock against pests of the mentioned type.
• compositions according to the invention are active against ectoparasites such as hard ticks, soft ticks, mange mites, harvest mites, flies (biting and licking), parasitic fly larvae, lice, hair lice, bird lice and fleas.
• ectoparasites such as hard ticks, soft ticks, mange mites, harvest mites, flies (biting and licking), parasitic fly larvae, lice, hair lice, bird lice and fleas.
• Anoplurida Haematopinus spp., Linognathus spp., Pediculus spp. and Phtirus spp., Solenopotes spp.
• Nematocerina and Brachycerina for example Aedes spp., Anopheles spp., Culex spp., Simulium spp., Eusimulium spp., Phlebotomus spp., Lutzomyia spp., Culicoides spp., Chrysops spp., Hybomitra spp., Atylotus spp., Tabanus spp., Haematopota spp., Philipomyia spp., Braula spp., Musca spp., Hydrotaea spp., Stomoxys spp., Haematobia spp., Morellia spp., Fannia spp., Glossina spp., Calliphora spp., Glossina spp., Calliphora spp., Glossina spp., Call
• Siphonapta for example Pulex spp., Ctenocephalides spp., Xenopsylla spp., Ceratophyllus spp.
• Heteropterida for example Cimex spp., Triatoma spp., Rhodnius spp., Panstrongylus spp.
• Blattarida for example Blatta orientalis, Periplaneta americana, Blattelagermanica and Supella spp.
• Actinedida Prostigmata
• Acaridida Acaridida
• Acarapis spp. Cheyletiella spp., Ornitrocheyletia spp., Myobia spp., Psorergates spp., Demodex spp., Trombicula spp., Listrophorus spp., Acarus spp., Tyrophagus spp., Caloglyphus spp., Hypodectes spp., Pterolichus spp., Psoroptes spp., Chorioptes spp., Otodectes spp., Sarcoptes spp., Notoedres spp., Knemidocoptes spp., Cytodites spp. and Laminosioptes spp.
• compositions according to the invention are also suitable for protecting against insect infestation in the case of materials such as wood, textiles, plastics, adhesives, glues, paints, paper and card, leather, floor coverings and buildings.
• compositions according to the invention can be used, for example, against the following pests: beetles such as Hylotrupes bajulus, Chlorophorus pilosis, Anobium punctatum, Xestobium rufovillosum, Ptilinuspecticornis, Dendrobium pertinex, Ernobius mollis, Priobium carpini, Lyctus brunneus, Lyctus africanus, Lyctus planicollis, Lyctus linearis, Lyctus pubescens, Trogoxylon aequale, Minthesrugicollis, Xyleborus spec., Tryptodendron spec., Apate monachus, Bostrychus capucins, Heterobostrychus brunneus, Sinoxylon spec.
• hymenopterans such as Sirex juvencus, Urocerus gigas, Urocerus gigas taignus and Urocerus augur , and termites such as Kalotermes flavicollis, Cryptotermes brevis, Heterotermes indicola, Reticulitermes flavipes, Reticulitermes santonensis, Reticulitermes lucifugus, Mastotermes darwiniensis, Zootermopsis nevadensis and Coptotermes formosanus , and bristletails such as Lepisma saccharina.
• the invention therefore also relates to pesticidal compositions such as emulsifiable concentrates, suspension concentrates, directly sprayable or dilutable solutions, spreadable pastes, dilute emulsions, soluble powders, dispersible powders, wettable powders, dusts, granules or encapsulations in polymeric substances, which comprise—at least—one of the active ingredients according to the invention and which are to be selected to suit the intended aims and the prevailing circumstances.
• pesticidal compositions such as emulsifiable concentrates, suspension concentrates, directly sprayable or dilutable solutions, spreadable pastes, dilute emulsions, soluble powders, dispersible powders, wettable powders, dusts, granules or encapsulations in polymeric substances, which comprise—at least—one of the active ingredients according to the invention and which are to be selected to suit the intended aims and the prevailing circumstances.
• the active ingredient is employed in pure form, a solid active ingredient for example in a specific particle size, or, preferably, together with—at least—one of the auxiliaries conventionally used in the art of formulation, such as extenders, for example solvents or solid carriers, or such as surface-active compounds (surfactants).
• auxiliaries conventionally used in the art of formulation, such as extenders, for example solvents or solid carriers, or such as surface-active compounds (surfactants).
• suitable solvents are: unhydrogenated or partially hydrogenated aromatic hydrocarbons, preferably the fractions C 8 to C 12 of alkylbenzenes, such as xylene mixtures, alkylated naphthalenes or tetrahydronaphthalene, aliphatic or cycloaliphatic hydrocarbons, such as paraffins or cyclohexane, alcohols such as ethanol, propanol or butanol, glycols and their ethers and esters such as propylene glycol, dipropylene glycol ether, ethylene glycol or ethylene glycol monomethyl ether or ethylene glycol monoethyl ether, ketones, such as cyclohexanone, isophorone or diacetone alcohol, strongly polar solvents, such as N-methylpyrrolid-2-one, dimethyl sulfoxide or N,N-dimethylformamide, water, unepoxidized or epoxidized vegetable oils, such as unexpodized or e
• Solid carriers which are used for example for dusts and dispersible powders are, as a rule, ground natural minerals such as calcite, talc, kaolin, montmorillonite or attapulgite.
• ground natural minerals such as calcite, talc, kaolin, montmorillonite or attapulgite.
• highly disperse silicas or highly disperse absorbtive polymers are also possible to add highly disperse silicas or highly disperse absorbtive polymers.
• Suitable particulate adsorptive carriers for granules are porous types, such as pumice, brick grit, sepiolite or bentonite, and suitable non-sorptive carrier materials are calcite or sand.
• a large number of granulated materials of inorganic or organic nature can be used, in particular dolomite or comminuted plant residues.
• Suitable surface-active compounds are, depending on the type of the active ingredient to be formulated, non-ionic, cationic and/or anionic surfactants or surfactant mixtures which have good emulsifying, dispersing and wetting properties.
• the surfactants mentioned below are only to be considered as examples; a large number of further surfactants which are conventionally used in the art of formulation and suitable according to the invention are described in the relevant literature.
• Suitable non-ionic surfactants are, especially, polyglycol ether derivatives of aliphatic or cycloaliphatic alcohols, of saturated or unsaturated fatty acids or of alkyl phenols which may contain approximately 3 to approximately 30 glycol ether groups and approximately 8 to approximately 20 carbon atoms in the (cyclo)aliphatic hydrocarbon radical or approximately 6 to approximately 18 carbon atoms in the alkyl moiety of the alkyl phenols.
• water-soluble polyethylene oxide adducts with polypropylene glycol, ethylenediaminopolypropylene glycol or alkyl polypropylene glycol having 1 to approximately 10 carbon atoms in the alkyl chain and approximately 20 to approximately 250 ethylene glycol ether groups and approximately 10 to approximately 100 propylene glycol ether groups.
• the abovementioned compounds contain 1 to approximately 5 ethylene glycol units per propylene glycol unit.
• nonylphenoxypolyethoxyethanol castor oil polyglycol ether, polypropylene glycol/polyethylene oxide adducts, tributylphenoxypolyethoxyethanol, polyethylene glycol or octylphenoxypolyethoxyethanol.
• fatty acid esters of polyoxyethylene sorbitan such as polyoxyethylene sorbitan trioleate.
• the cationic surfactants are, especially, quarternary ammonium salts which generally have at least one alkyl radical of approximately 8 to approximately 22 C atoms as substituents and as further substituents (unhalogenated or halogenated) lower alkyl or hydroxyalkyl or benzyl radicals.
• the salts are preferably in the form of halides, methylsulfates or ethylsulfates. Examples are stearyltrimethylammonium chloride and benzylbis(2-chloroethyl)ethylammonium bromide.
• Suitable anionic surfactants are water-soluble soaps or water-soluble synthetic surface-active compounds.
• suitable soaps are the alkali, alkaline earth or (unsubstituted or substituted) ammonium salts of fatty acids having approximately 10 to approximately 22 C atoms, such as the sodium or potassium salts of oleic or stearic acid, or of natural fatty acid mixtures which are obtainable for example from coconut or tall oil; mention must also be made of the fatty acid methyl taurates.
• synthetic surfactants are used more frequently, in particular fatty sulfonates, fatty sulfates, sulfonated benzimidazole derivatives or alkylaryl sulfonates.
• the fatty sulfonates and fatty sulfates are present as alkali, alkaline earth or (substituted or unsubstituted) ammonium salts and they generally have an alkyl radical of approximately 8 to approximately 22 C atoms, alkyl also to be understood as including the alkyl moiety of acyl radicals; examples which may be mentioned are the sodium or calcium salts of lignosulfonic acid, of the dodecylsulfuric ester or of a fatty alcohol sulfate mixture prepared from natural fatty acids. This group also includes the salts of the sulfuric esters and sulfonic acids of fatty alcohol/ethylene oxide adducts.
• the sulfonated benzimidazole derivatives preferably contain 2 sulfonyl groups and a fatty acid radical of approximately 8 to approximately 22 C atoms.
• alkylarylsulfonates are the sodium, calcium or triethanolammonium salts of decylbenzenesulfonic acid, of dibutylnaphthalenesulfonic acid or of a naphthalenesulfonic acid/formaldehyde condensate.
• suitable phosphates such as salts of the phosphoric ester of a p-nonylphenol/(4-14)ethylene oxide adduct, or phospholipids.
• the compositions comprise 0.1 to 99%, especially 0.1 to 95%, of active ingredient and 1 to 99.9%, especially 5 to 99.9%, of at least one solid or liquid adjuvant, it being possible as a rule for 0 to 25%, especially 0.1 to 20%, of the composition to be surfactants (% in each case meaning percent by weight).
• surfactants % in each case meaning percent by weight.
• concentrated compositions tend to be preferred for commercial goods
• dilute compositions which have substantially lower concentrations of active ingredient.
• active ingredient 1 to 95%, preferably 5 to 20% surfactant: 1 to 30%, preferably 10 to 20% solvent: 5 to 98%, preferably 70 to 85% Dusts:
• active ingredient 5 to 75%, preferably 10 to 50% water: 94 to 24%, preferably 88 to 30% surfactant: 1 to 40%, preferably 2 to 30% Wettable Powders:
• active ingredient 0.5 to 90%, preferably 1 to 80% surfactant: 0.5 to 20%, preferably 1 to 15% solid carrier: 5 to 99%, preferably 15 to 98% Granulates:
• active ingredient 0.5 to 30%, preferably 3 to 15% solid carrier: 99.5 to 70%, preferably 97 to 85%
• the precipitate is collected by filtration, washed with water, dissolved in dichloromethane and washed with water. After drying, filtering off the drying agent and evaporation of the solvent, die crude product is passed through a short column to give a mixture of two nitro isomers which are not separated but used directly in the next stage.
• reaction mixture is then stirred for 15 hours, then poured onto ice-water, the solid filtered, washed with water and dried to give 5-chloro-7-[2-(3-chloro-pyridin-2-yl)-5-trifluoromethyl-2H-pyrazole-3-carbonyl]-1,3-(2′2′difluoro)dioxolane-8-oxa-naphthalen-9-one as a solid with melting point 198-200° C.
• reaction mixture is then stirred for 15 hours, then poured onto ice-water, the solid filtered, washed with water and dried to give 5-methyl-7-[2-(3-chloro-pyridin-2-yl)-5-bromo-2H-pyrazole-3-carbonyl]-1,3-(2′2′difluoro)dioxolane-8-oxa-naphthalen-9-one as a solid with melting point 223-225° C.
• This compound is prepared as described in the U.S. Pat. No. 0,167,128 A1, 2004.
• 6-amino-7-bromoindanone 2.4 g, 10.6 mmol
• sodium borohydride 360 mg, 10.6 mmol
• Tetrahydrofuran is evaporated and the residue is dissolved in ethyl acetate and washed with water.
• the separated organic layer is dried over sodium sulfate, filtered, and evaporated to give 6-amino-7-bromoindan-1-ol; GC/MS: 228/230 (M+1) + .
• a suspension of 6-iodo-3,4-dioxolane-(di-N-tert-butyloxycarbonyl)-anthranilic acid methyl ester (0.1 g, 0.019 mmol), potassium carbonate (0.026 g, 0.019 mmol), tetrakis(triphenyl phosphine)palladium (1 mol %) and trimethylboraxine (0.026 ml, 0.019 mmol) in 1,4-dioxane (5 ml) is stirred under nitrogen at 105° C. for 10 hours. Solvent is removed and the residue is taken in ethyl acetate (50 ml).
• Table 1 This table discloses the 706 compounds T1.1.1 to T1.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• the specific compound T1.1.23 is the compound of the formula T1, in which each of the variables R 1a , R 20 and R 100 has the specific meaning given in the line A.1.23 of the Table A.
• all of the other 706 specific compounds disclosed in the Table 1 as well as all of the specific compounds disclosed in the Tables 2 to 55 are specified analogously.
• Table 2 This table discloses the 706 compounds T2.1.1 to T2.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 564 lines A.1.1 to A.1.706 of the Table A.
• Table 3 This table discloses the 706 compounds T3.1.1 to T3.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 4 This table discloses the 706 compounds T4.1.1 to T4.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 5 This table discloses the 706 compounds T5.1.1 to T5.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 6 This table discloses the 706 compounds T6.1.1 to T6.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 7 This table discloses the 706 compounds T7.1.1 to T7.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 8 This table discloses the 706 compounds T8.1.1 to T8.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 9 This table discloses the 706 compounds T9.1.1 to T9.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 10 This table discloses the 706 compounds T10.1.1 to T10.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 11 This table discloses the 706 compounds T11.1.1 to T11.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 12 This table discloses the 706 compounds T12.1.1 to T12.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 13 This table discloses the 706 compounds T13.1.1 to T13.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 14 This table discloses the 706 compounds T14.1.1 to T14.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 15 This table discloses the 706 compounds T15.1.1 to T15.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 16 This table discloses the 706 compounds T16.1.1 to T16.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 17 This table discloses the 706 compounds T17.1.1 to T17.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 18 This table discloses the 706 compounds T18.1.1 to T18.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1706 of the Table A.
• Table 19 This table discloses the 706 compounds T19.1.1 to T19.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 20 This table discloses the 706 compounds T20.1.1 to T20.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 21 This table discloses the 706 compounds T21.1.1 to T21.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 22 This table discloses the 706 compounds T22.1.1 to T22.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 23 This table discloses the 706 compounds T23.1.1 to T23.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 24 This table discloses the 706 compounds T24.1.1 to T24.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 25 This table discloses the 706 compounds T25.1.1 to T25.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 26 This table discloses the 706 compounds T26.1.1 to T26.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, approximately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 27 This table discloses the 706 compounds T27.1.1 to T27.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 28 This table discloses the 706 compounds T28.1.1 to T28.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 29 This table discloses the 706 compounds T29.1.1 to T29.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 30 This table discloses the 706 compounds T30.1.1 to T30.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 31 This table discloses the 706 compounds T31.1.1 to T31.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 32 This table discloses the 706 compounds T32.1.1 to T32.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 33 This table discloses the 706 compounds T33.1.1 to T33.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 34 This table discloses the 706 compounds T34.1.1 to T34.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 35 This table discloses the 706 compounds T35.1.1 to T35.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 36 This table discloses the 706 compounds T36.1.1 to T36.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 37 This table discloses the 706 compounds T37.1.1 to T37.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 38 This table discloses the 706 compounds T38.1.1 to T38.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 39 This table discloses the 706 compounds T39.1.1 to T39.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 40 This table discloses the 706 compounds T40.1.1 to T40.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 41 This table discloses the 706 compounds T41.1.1 to T41.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 42 This table discloses the 706 compounds T42.1.1 to T42.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 43 This table discloses the 706 compounds T43.1.1 to T43.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 44 This table discloses the 706 compounds T44.1.1 to T44.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 45 This table discloses the 706 compounds T45.1.1 to T45.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 46 This table discloses the 706 compounds T46.1.1 to T46.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 47 This table discloses the 706 compounds T47.1.1 to T47.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 48 This table discloses the 706 compounds T48.1.1 to T48.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 49 This table discloses the 706 compounds T49.1.1 to T49.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 50 This table discloses the 706 compounds T50.1.1 to T50.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 51 This table discloses the 706 compounds T51.1.1 to T51.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 52 This table discloses the 706 compounds T52.1.1 to T52.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 53 This table discloses the 706 compounds T53.1.1 to T53.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 54 This table discloses the 706 compounds T54.1.1 to T54.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 55 This table discloses the 706 compounds T55.1.1 to T55.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 56 This table discloses the 706 compounds T56.1.1 to T56.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Table 57 This table discloses the 706 compounds T57.1.1 to T57.1.706 of the formula
• each of the of the variables R 1a , R 20 and R 100 has the specific meaning given in the corresponding line, appropriately selected from the 706 lines A.1.1 to A.1.706 of the Table A.
• Emulsion concentrates a) b) c) Active ingredient 25% 40% 50% Calcium dodecylbenzenesulfonate 5% 8% 6% Castor oil polyethylene glycol ether (36 mol of EO) 5% — — Tributylphenoxypolyethylene glycol ether — 12% 4% (30 mol of EO) Cyclohexanone — 15% 20% Xylene mixture 65% 25% 20%
• Emulsions of any desired concentration can be prepared from such concentrates by dilution with water.
• the solutions are suitable for use in the form of microdrops.
• the active ingredient is dissolved in dichloromethane, the solution is sprayed onto the carrier(s), and the solvent is subsequently evaporated in vacuo.
• Ready-to-use dusts are obtained by intimately mixing the carriers and the active ingredient.
• Wettable powders a) b) c) Active ingredient 25% 50% 75% Sodium lignosulfonate 5% 5% — Sodium lauryl sulfate 3% — 5% Sodium diisobutylnaphthalenesulfonate — 6% 10% Octylphenoxypolyethylene glycol — 2% — ether (7-8 mol of EO) Highly disperse silica 5% 10% 10% Kaolin 62% 27% —
• the active ingredient is mixed with the additives and the mixture is ground thoroughly in a suitable mill. This gives wettable powders, which can be diluted with water to give suspensions of any desired concentration.
• the active ingredient is mixed with the additives, and the mixture is ground, moistened with water, extruded, granulated and dried in a stream of air.
• the finely ground active ingredient is applied uniformly to the kaolin, which has been moistened with the polyethylene glycol. This gives dust-free coated granules.
• Suspension concentrate Active ingredient 40% Ethylene glycol 10% Nonylphenoxypolyethylene glycol ether (15 mol of EO) 6% Sodium lignosulfonate 10% Carboxymethylcellulose 1% 37% aqueous formaldehyde solution 0.2% Silicone oil (75% aqueous emulsion) 0.8% Water 32%
• the finely ground active ingredient is mixed intimately with the additives.
• Suspensions of any desired concentration can be prepared from the thus resulting suspension concentrate by dilution with water.
• compositions according to the invention can be broadened considerably, and adapted to prevailing circumstances, by adding other insecticidally, acaricidally and/or fungicidally active ingredients.
• mixtures of the compounds of formula I with other insecticidally, acaricidally and/or fungicidally active ingredients may also have further surprising advantages which can also be described, in a wider sense, as synergistic activity. For example, better tolerance by plants, reduced phytotoxicity, insects can be controlled in their different development stages or better behaviour during their production, for example during grinding or mixing, during their storage or during their use.
• Suitable additions to active ingredients here are, for example, representatives of the is following classes of active ingredients: organophosphorus compounds, nitrophenol derivatives, thioureas, juvenile hormones, formamidines, benzophenone derivatives, ureas, pyrrole derivatives, carbamates, pyrethroids, chlorinated hydrocarbons, acylureas, pyridylmethyleneamino derivatives, macrolides, neonicotinoids and Bacillus thuringiensis preparations.
• TX means “one compound selected from the group consisting of the compounds of formulae T1 to T57 described in tables 1 to 57 of the present invention”.
• Ra 5 is trifluoromethyl or difluoromethyl (WO2004/058723)+TX, the compound of formula F-2
• Ra 6 is trifluoromethyl or difluoromethyl (WO2004/058723)+TX, the racemic compound of formula F-3 (syn)
• Ra 7 is trifluoromethyl or difluoromethyl (WO2004/035589)+TX, the racemic mixture of formula F-4 (anti)
• Ra 7 is trifluoromethyl or difluoromethyl (WO2004/035589)+TX, the compound of formula F-5
• Ra 8 is trifluoromethyl or difluoromethyl (WO2004/035589)+TX, the racemic compound of formula F-7 (trans)
• Ra 9 is trifluoromethyl or difluoromethyl (WO03/074491)+TX, the racemic compound of formula F-8 (cis)
• Ra 9 is trifluoromethyl or difluoromethyl (WO03/074491)+TX, the compound of formula F-9
• R 10 is trifluoromethyl or difluoromethyl (WO2004/058723)+TX, the racemic compound of formula F-11 (trans)
• R 11 is trifluoromethyl or difluoromethyl (WO03/074491)+TX, the racemic compound of formula F-12 (cis)
• R 11 is trifluoromethyl or difluoromethyl (WO03/074491)+TX, the compound of formula F-13
• the active ingredient mixture of the compounds of formula I selected from tables T1 to T57 with active ingredients described above comprises a compound selected from tables T1 to T57 and an active ingredient as described above preferably in a mixing ratio of from 100:1 to 1:6000, especially from 50:1 to 1:50, more especially in a ratio of from 20:1 to 1:20, even more especially from 10:1 to 1:10, very especially from 5:1 and 1:5, special preference being given to a ratio of from 2:1 to 1:2, and a ratio of from 4:1 to 2:1 being likewise preferred, above all in a ratio of 1:1, or 5:1, or 5:2, or 5:3, or 5:4, or 4:1, or 4:2, or 4:3, or 3:1, or 3:2, or 2:1, or 1:5, or 2:5, or 3:5, or 4:5, or 1:4, or 2:4, or 3:4, or 1:3, or 2:3, or 1:2, or 1:600, or 1:300, or 1:150, or 1:35, or 2:35, or 4:35, or 1:75, or
• the mixtures comprising a compound of formula I selected from tables T1 to T57 and one or more active ingredients as described above can be applied, for example, in a single “ready-mix” form, in a combined spray mixture composed from separate formulations of the single active ingredient components, such as a “tank-mix”, and in a combined use of the single active ingredients when applied in a sequential manner, i.e. one after the other with a reasonably short period, such as a few hours or days.
• the order of applying the compounds of formula I selected from tables T1 to T57 and the active ingredients as described above is not essential for working the present invention.
• compositions can also comprise further solid or liquid auxiliaries, such as stabilizers, for example unepoxidized or epoxidized vegetable oils (for example epoxidized coconut oil, rapeseed oil or soya oil), antifoams, for example silicone oil, preservatives, viscosity regulators, binders and/or tackifiers, fertilizers or other active ingredients for achieving specific effects, for example bactericides, fungicides, nematocides, plant activators, molluscicides or herbicides.
• auxiliaries such as stabilizers, for example unepoxidized or epoxidized vegetable oils (for example epoxidized coconut oil, rapeseed oil or soya oil), antifoams, for example silicone oil, preservatives, viscosity regulators, binders and/or tackifiers, fertilizers or other active ingredients for achieving specific effects, for example bactericides, fungicides, nematocides, plant activators
• compositions according to the invention are prepared in a manner known per se, in the absence of auxiliaries for example by grinding, screening and/or compressing a solid active ingredient and in the presence of at least one auxiliary for example by intimately mixing and/or grinding the active ingredient with the auxiliary (auxiliaries).
• auxiliaries for example by grinding, screening and/or compressing a solid active ingredient and in the presence of at least one auxiliary for example by intimately mixing and/or grinding the active ingredient with the auxiliary (auxiliaries).
• compositions that is the methods of controlling pests of the abovementioned type, such as spraying, atomizing, dusting, brushing on, dressing, scattering or pouring—which are to be selected to suit the intended aims of the prevailing circumstances—and the use of the compositions for controlling pests of the abovementioned type are other subjects of the invention.
• Typical rates of concentration are between 0.1 and 1000 ppm, preferably between 0.1 and 500 ppm, of active ingredient.
• the rate of application per hectare is generally 1 to 2000 g of active ingredient per hectare, in particular 10 to 1000 g/ha, preferably 10 to 600 g/ha.
• a preferred method of application in the field of crop protection is application to the foliage of the plants (foliar application), it being possible to select frequency and rate of application to match the danger of infestation with the pest in question.
• the active ingredient can reach the plants via the root system (systemic action), by drenching the locus of the plants with a liquid composition or by incorporating the active ingredient in solid form into the locus of the plants, for example into the soil, for example in the form of granules (soil application). In the case of paddy rice crops, such granules can be metered into the flooded paddy-field.
• compositions according to the invention are also suitable for the protection of plant propagation material, for example seeds, such as fruit, tubers or kernels, or nursery plants, against pests of the abovementioned type.
• the propagation material can be treated with the compositions prior to planting, for example seed can be treated prior to sowing.
• the compositions can be applied to seed kernels (coating), either by soaking the kernels in a liquid composition or by applying a layer of a solid composition. It is also possible to apply the compositions when the propagation material is planted to the site of application, for example into the seed furrow during drilling.
• Cotton leaf discs are placed on agar in a 24-well microtiter plate and sprayed with test solutions. After drying, the leaf discs are infested with 5 L 1 larvae. The samples are checked for mortality, repellent effect, feeding behaviour, and growth regulation 3 days after treatment. In this test, compounds listed in Table P above show good activity.
• Eggs (0-24 h old) are placed in 24-well microtiter plate on artificial diet and treated with test solutions by pipetting. After an incubation period of 4 days, samples are checked for egg mortality, larval mortality, and growth regulation.
• MTP 24-well microtiter plate
• L2 larvae
• MTP 24-well microtiter plate
• L2 larvae
• compounds listed in Table P above show good activity.
• Sunflower leaf discs are placed on agar in a 24-well microtiter plate and sprayed with test solutions. After drying, the leaf discs are infested with an aphid population of mixed ages. After an incubation period of 6 days, samples are checked for mortality and special effects (e.g. phytotoxicity).
• compounds listed in Table P above show good activity.
• compounds P.5, P.12, P.14, P.15, P.16, P.18, P.19, P.20, P.21, P.22, P.23, P.24, P.26, P.27, P.30, P.31, P.71, P.83 and P.88 show an activity of over 80% at a concentration of 400 ppm.
• Roots of pea seedlings, infested with an aphid population of mixed ages, are placed directly in the test solutions. 6 days after introduction, samples are checked for mortality and special effects on the plant.
• Sunflower leaf discs are placed on agar in a 24-well microtiter plate and sprayed with test solutions. After drying, the leaf discs are infested with a thrips population of mixed ages. After an incubation period of 6 days, samples are checked for mortality and special effects (e.g. phytotoxicity).
• MTP 24-well microtiter plate
• L2 larvae
• Table B8 shows that compound No. P.13 according to the invention exerts a substantially better insecticidal action on Plutella xylostella than the compound from the state of the art. Especially at low application rates (12.5, 3.1 and 0.8 ppm) the compound according to the invention is far superior to the compound of the state of the art. This enhanced effect was not to be expected on the basis of the structural similarity of these compounds.
• Cotton leaf discs are placed on agar in a 24-well microtiter plate and sprayed with test solutions. After drying, the leaf discs are infested with 5 L 1 larvae. The samples are checked for mortality, repellent effect, feeding behaviour, and growth regulation 3 days after treatment.
• Table B9 shows that compound No. P.13 according to the invention exerts a substantially better insecticidal action on Spodoptera littoralis than the compound from the state of the art. Especially at low application rates (12.5, 3.1 and 0.8 ppm) the compound according to the invention is far superior to the compound of the state of the art. This enhanced effect was not to be expected on the basis of the structural similarity of these compounds.

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